Integra LifeSciences is a global leader in regenerative technologies and neurosurgical solutions dedicated to limiting uncertainty for clinicians, so they can focus on providing the best patient care.

Founded in 1989, Integra develops, manufactures, sells and supplies best-in-class products to regenerate tissue, remove brain tumors, prevent infection and much more. And over the last three decades, we’ve evolved into one of the world’s leading global medical technology companies with more than 4,000 dedicated employees who deliver innovative medical technology solutions.


But that’s just the beginning. Integra is growing at an unprecedented rate. We’re at a moment in time where the experience you’ll gain is more robust than the experience you bring. And we’re out to invest in your future because it’s the best way to maximize ours.

Ingénieur qualité

Integra LifeSciences is a global leader in regenerative technologies and neurosurgical solutions dedicated to limiting uncertainty for clinicians, so they can focus on providing the best patient care.

Founded in 1989, Integra develops, manufactures, sells and supplies best-in-class products to regenerate tissue, remove brain tumors, prevent infection and much more. And over the last three decades, we’ve evolved into one of the world’s leading global medical technology companies with more than 4,000 dedicated employees who deliver innovative medical technology solutions.


But that’s just the beginning. Integra is growing at an unprecedented rate. We’re at a moment in time where the experience you’ll gain is more robust than the experience you bring. And we’re out to invest in your future because it’s the best way to maximize ours.

    • Quality support for production and for various projects
    • Plan, coordinate and direct the quality aspects of process validation
    • Write validation documentation (protocols, reports, process specifications, work instructions, pFMEA, master validation plan)
    • Provide projects updates and presentations
    • Review and approve changes to documentation and processes
    • Apply and enforce GMP
    • Non-conformance management (initiation / evaluation / disposition on the batches / investigation)
    • Quality control technical support
    • Participation in development and updating of procedures and other quality documents
    • Participation in validations of new processes (Processes, products, methods & software)
    • Validation of different integrated processes